rs1060502482

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs1060502482(-;-)

Make rs1060502482(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

32356439

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs1060502482
dbSNP (classic)	rs1060502482
ClinGen	rs1060502482
ebi	rs1060502482
HLI	rs1060502482
Exac	rs1060502482
Gnomad	rs1060502482
Varsome	rs1060502482
LitVar	rs1060502482
Map	rs1060502482
PheGenI	rs1060502482
Biobank	rs1060502482
1000 genomes	rs1060502482
hgdp	rs1060502482
ensembl	rs1060502482
geneview	rs1060502482
scholar	rs1060502482
google	rs1060502482
pharmgkb	rs1060502482
gwascentral	rs1060502482
openSNP	rs1060502482
23andMe	rs1060502482
SNPshot	rs1060502482
SNPdbe	rs1060502482
MSV3d	rs1060502482
GWAS Ctlg	rs1060502482

Max Magnitude

0

ClinVar
Risk	rs1060502482(-;-)
Alt	rs1060502482(-;-)
Reference	Rs1060502482(A;A)
Significance	Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32930576delA
CLNSRC
CLNACC	RCV000461479.1,